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Molecular signaling pathways triggered by rituximab: prognostic, diagnostic, and therapeutic uses

a technology of molecular signaling pathways and rituximab, which is applied in the direction of instruments, biochemistry apparatus and processes, material analysis, etc., can solve the problems of not explaining the enhanced response achieved with the treatment combination of rituximab and chemotherapeutic drugs, and the failure of approximately 50% of nhl patients to respond, so as to regulate the sensitivity of cancer cells to immunotherapy

Inactive Publication Date: 2009-08-13
RGT UNIV OF CALIFORNIA
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  • Abstract
  • Description
  • Claims
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AI Technical Summary

Benefits of technology

The approach enhances the sensitivity of NHL cells to chemotherapeutic drugs and immunotherapy by modulating key signaling pathways, reversing drug resistance and improving treatment outcomes.

Problems solved by technology

However, these postulated mechanisms do not explain the failure of approximately 50% of NHL patients to respond to rituximab treatment alone and do not explain the enhanced response achieved with treatment combination of rituximab and chemotherapeutic drugs in patients with drug-resistant tumors.

Method used

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  • Molecular signaling pathways triggered by rituximab: prognostic, diagnostic, and therapeutic uses
  • Molecular signaling pathways triggered by rituximab: prognostic, diagnostic, and therapeutic uses
  • Molecular signaling pathways triggered by rituximab: prognostic, diagnostic, and therapeutic uses

Examples

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example 1

Regulation of Chemoresistance and Immune Resistance of B-NHL Cell Lines by Overexpression of YY1 and Bcl-xl, Respectively: Reversal of Resistance by Rituximab

[0226]We have recently reported that treatment of B-Non-Hodgkin's Lymphoma (NHL) cell lines with rituximab (anti-CD20 antibody) sensitizes the tumor cells to both chemotherapy and Fas-induced apoptosis (Jazirehi and Bonavida, Oncogene, 24:2121-2145 (2005)). This study investigated the underlying molecular mechanism of rituximab-mediated reversal of immune and drug resistance. Treatment of B-NHL cell lines inhibited the constitutively activated NF-κB. Cells expressing dominant active IicB or treated with NF-κB specific inhibitors were sensitized to both drugs and FasL agonist mAb (CH-11)-induced apoptosis. Downregulation of Bcl-XL expression via inhibition of NF-κB activity correlated with chemosensitivity. The direct role of Bcl-XL in chemoresistance was demonstrated by the use of Bcl-XL overexpressing Ramos cells, Ramos HA-Bcl...

example 2

Rituximab-Mediated Inhibition of the Transcription Repressor Yin-Yang 1 (YY1) in NHL B Cell Lines: Upregulation of Fas Expression and Sensitization to Fas-Induced Apoptosis

[0227]We have reported that rituximab triggers and inhibits anti-apoptotic gene products in NHL B-cell lines resulting in sensitization to drug-induced apoptosis (Alas et al., Clin. Cancer Res., 8:836 (2001); Jazirehi et al., Mol. Cancer Therapy, 2:1183 (2003); Vega et al., Oncogene, 23:3530 (2004)). This study investigated whether rituximab also modifies intracellular signaling pathways resulting in the sensitization of NHL cells to Fas-induced apoptosis. Treatment of the NHL cell lines (2F7, Ramos, and Raji) with rituximab (20 μg / ml) sensitized the cells to CH-11 (FasL agonist mAb)-induced apoptosis and synergy was achieved. Fas expression was up-regulated by rituximab as early as 6 h post treatment as determined by flow cytometry, RT-PCR, and Western. Rituximab inhibited both the expression and activity of the ...

example 3

Rituximab Diminishes the Constitutive Activity of the PI3k-Akt Signaling Pathway in Ramos B-NHL Cells

[0228]Rituximab (chimeric anti-CD20 monoclonal antibody) is currently being used, alone or in combination with chemotherapy, in the treatment of B-Non Hodgkin's Lymphoma (B-NHL). We have reported that rituximab treatment of B-NHL cell lines sensitizes the drug-resistant tumor cells to apoptosis by various chemotherapeutic drugs and chemosensitization was due, in large part, to the selective inhibition of the anti-apoptotic Bcl-XL gene product. The constitutive activation of the Akt pathway in B-NHL results in overexpression and functional activation of Bcl-XL. The hypothesis that the rituximab-induced inhibition of Bcl-XL expression and chemosensitization resulted, in part, from its inhibitory activity of the Akt pathway was tested using the drug-resistant Ramos B-NHL cell line. Time kinetic analysis revealed that treatment of Ramos with rituximab inhibited phosphorylation of Akt (p-...

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Abstract

The present invention provides markers associated with activated molecular signaling pathways (example: p38 MAKP, NF-κB, ERK1 / 2, YY-1 and AKT) inhibited by rituximab in cancer cells as well as pathways activated by rituximab (such as death receptors, RKIP, PTEN) all of which are associated with the regulation of chemo and immunoresistance. The present invention provides methods of prognosis and providing a prognosis for cancer such as lymphoma, leukemia, and autoimmune disease, as well as, methods of drug discovery. These markers are also therapeutic targets for treatment of cancer resistant to conventional and experimental cancer therapeutics. Inhibition or activation of expression and / or activity of targeted gene products sensitizes resistant tumor cells to subtoxic doses of cytotoxic treatment including chemotherapy, radiation therapy, or immunotherapy and gene therapy, and the cytotoxic molecules.

Description

STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT[0001]This invention was made with Government support under Department of Defense / US Army Grant DAMD 17-02-1-0023. The Government has certain rights in this invention.CROSS-REFERENCES TO RELATED APPLICATIONS[0002]Not applicable.BACKGROUND OF THE INVENTION[0003]Cancer is the second leading cause of death behind heart disease. Cancer incidence and death figures account for about 10% of the U.S. population in certain areas of the United States (National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) database and Bureau of the Census statistics; see, Harrison's Principles of Internal Medicine, Kasper et al., 16th ed., 2005, Chapter 66). The five leading causes of cancer deaths among men are lung cancer, prostate cancer, colon and rectum cancer, pancreatic cancer and leukemias. The five leading causes of cancer deaths among women are lung cancer, breast cancer, colon cancer, ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/7088G01N33/53C12Q1/68
CPCG01N33/57426G01N33/5088
Inventor BONAVIDA, BENJAMINJAZIREHI, ALI R.
Owner RGT UNIV OF CALIFORNIA
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